Senior Clinical Research Associate (CRA)
About this role
About the Role Senior Clinical Research Associate to oversee and manage clinical trial activities at ICON, ensuring studies run according to protocol, regulatory requirements, and GCP standards, with focus on data integrity and participant safety throughout the study lifecycle. What You'll Do
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
- Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
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